SREK1 and HNRNPU

  • Number of citations of the paper that reports this interaction (PMID 14559993)
  • 9
  • Data Source:
  • HPRD (in vivo, two hybrid, in vitro)

SREK1

HNRNPU

Gene Name splicing regulatory glutamine/lysine-rich protein 1 heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A)
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 55 interactors: CD8A CSNK2A1 DDX17 DDX39B DDX3X DGKA DGKD EFTUD2 ELAVL1 GNB2L1 HNRNPA1 HNRNPA2B1 HNRNPA3 HNRNPC HNRNPD HNRNPH1 HNRNPK HNRNPU ILF2 MDM2 NCL NPM1 PABPC1 PABPC4 PARP1 PIN1 RBM10 RBMX SAFB SF3A3 SF3B3 SFPQ SH3GLB2 SNRPD1 SNRPD3 SRPK1 SRPK2 SRPK3 SRSF1 SRSF10 SRSF11 SRSF2 SRSF3 SRSF4 SRSF5 SRSF6 SRSF7 SRSF8 SSRP1 SUPT16H TARBP1 THRAP3 TRA2B YBX1 ZRANB2 35 interactors: ACTB BTRC CASP3 CD5 CDKN2A CR2 ELL EP300 ERG GAS7 GRIN1 GRIN2D GTF2H1 HNRNPD HNRNPH3 IL7R KAT2B NDN NDRG1 NEDD4 NR3C1 PIN1 POLR2A POU3F4 PRMT1 PRPF40A PTPN11 SMN1 SREK1 STAU1 SYK TCERG1 WBP4 YAP1 ZNF689
Entrez ID 140890 3192
HPRD ID 18043 04185
Ensembl ID ENSG00000153914 ENSG00000153187
Uniprot IDs E5RFV3 Q8WXA9 Q00839 Q96BA7
PDB IDs 1ZRJ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17p13  1q21  1q44  2q23  2q31  agilent  annotations  asd  autism  backgrounds  cgh  cnv  cnvs  disabilities  dissect  encephalopathy  epileptic  exome  expand  hallux  implicates  infantile  intellectual  lissencephaly  mbd5  microcephaly  pafah1b1  pathogenicity  spasms 
Tagcloud (Difference) ?
17p13  1q21  1q44  2q23  2q31  agilent  annotations  asd  autism  backgrounds  cgh  cnv  cnvs  disabilities  dissect  encephalopathy  epileptic  exome  expand  hallux  implicates  infantile  intellectual  lissencephaly  mbd5  microcephaly  pafah1b1  pathogenicity  spasms 
Tagcloud (Intersection) ?